HGVS | Genome Assembly |
---|---|
NC_000010.11:g.14436590A>G , CM000672.2:g.14436590A>G | GRCh38 |
NC_000010.10:g.14478589A>G , CM000672.1:g.14478589A>G | GRCh37 |
NC_000010.9:g.14518595A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000475141.2:c.-305+25478T>C (FRMD4A) | ENSP00000473870.1:n.-305+25478T>C | |
ENST00000493380.5:c.-82+25478T>C (FRMD4A) | ENSP00000474863.1:n.-82+25478T>C | |
NR_031668.1:n.15A>G (MIR1265) |